rs7534785

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0064 (1914/29834,GnomAD)
A=0072 (2111/29116,TOPMED)
A=0108 (543/5008,1000G)
A=0028 (106/3854,ALSPAC)
A=0026 (95/3708,TWINSUK)
chr1:214929079 (GRCh38.p7) (1q41)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.214929079G>A
GRCh37.p13 chr 1NC_000001.10:g.215102422G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.896A=0.104
1000GenomesAmericanSub694G=0.940A=0.060
1000GenomesEast AsianSub1008G=0.809A=0.191
1000GenomesEuropeSub1006G=0.971A=0.029
1000GenomesGlobalStudy-wide5008G=0.892A=0.108
1000GenomesSouth AsianSub978G=0.860A=0.140
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.972A=0.028
The Genome Aggregation DatabaseAfricanSub8686G=0.890A=0.110
The Genome Aggregation DatabaseAmericanSub838G=0.950A=0.050
The Genome Aggregation DatabaseEast AsianSub1610G=0.803A=0.197
The Genome Aggregation DatabaseEuropeSub18398G=0.968A=0.031
The Genome Aggregation DatabaseGlobalStudy-wide29834G=0.935A=0.064
The Genome Aggregation DatabaseOtherSub302G=0.950A=0.050
Trans-Omics for Precision MedicineGlobalStudy-wide29116G=0.927A=0.072
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.974A=0.026
PMID Title Author Journal
21314694Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.Kendler KSAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs75347850.000529alcohol dependence21314694

eQTL of rs7534785 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs7534785 in Fetal Brain

Probe ID Position Gene beta p-value
There is no meQTL annotation for this SNP

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr1215139752215140020E06737330
chr1215139752215140020E06837330
chr1215139752215140020E06937330
chr1215071003215071283E070-31139
chr1215139752215140020E07237330
chr1215139752215140020E07437330
chr1215069237215069287E081-33135
chr1215070022215070749E081-31673
chr1215071003215071283E081-31139
chr1215071580215071845E081-30577
chr1215072271215072312E081-30110
chr1215085536215085834E081-16588
chr1215085959215086228E081-16194
chr1215086243215086440E081-15982
chr1215069237215069287E082-33135
chr1215070022215070749E082-31673
chr1215071003215071283E082-31139
chr1215071580215071845E082-30577
chr1215085536215085834E082-16588
chr1215085959215086228E082-16194
chr1215086243215086440E082-15982
chr1215087379215087564E082-14858